A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18144435



Internal ID20711475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70296854..70297275hg38UCSC Ensembl
chr6:71006557..71006978hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402120
Supporting Variants
Samples
Known GenesCOL9A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18144435
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00298


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